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植物源性食品中氟吡菌、烯肟菌、氯虫苯甲酰残留的LC-MS/MS检测方法研究
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  • 英文篇名:Determination method of fluopicolide,fenaminstrobin and chlorantraniliprole residues in plant foods by LC-MS/MS
  • 作者:司文帅 ; 张颖 ; 张其才 ; 韩奕奕 ; 杨晓君 ; 白冰 ; 宋卫国
  • 英文作者:SI Wen-shuai;ZHANG Ying;ZHANG Qi-cai;HAN Yi-yi;YANG Xiao-jun;BAI Bing;SONG Wei-guo;Institute for Agro-Food Standards and Testing Technology,Shanghai Academy of Agricultural Sciences;Shanghai University of Medicine & Health Sciences;Agri-products Quality and Safety Testing Center of Shanghai;
  • 关键词:植物源性食品 ; 氟吡菌 ; 烯肟菌 ; 氯虫苯甲酰 ; 液相色谱-串联质谱
  • 英文关键词:Plant foods;;Fluopicolide;;Fenaminstrobin;;Chlorantraniliprole;;Liquid chromatographytandem mass spectrometry(LC-MS/MS)
  • 中文刊名:SHLB
  • 英文刊名:Acta Agriculturae Shanghai
  • 机构:上海市农业科学院农产品质量标准与检测技术研究所;上海健康医学院;上海市农产品质量安全检测中心;
  • 出版日期:2019-01-30
  • 出版单位:上海农业学报
  • 年:2019
  • 期:v.35
  • 基金:上海市农委科技兴农重点攻关项目[沪农科攻字(2015)第4-7号];; 上海市市级农口系统青年人才成长计划[沪农青字(2016)第1-25号];; 上海市科委长三角合作项目(16395810400)
  • 语种:中文;
  • 页:SHLB201901015
  • 页数:4
  • CN:01
  • ISSN:31-1405/S
  • 分类号:81-84
摘要
采用液相色谱-串联质谱仪(LC-MS/MS)建立了植物源性食品中氟吡菌、烯肟菌、氯虫苯甲酰残留的定量分析方法,样品经过乙腈涡旋提取后,无水MgSO4、PSA和C18分散固相萃取净化,LC-MS/MS检测。结果表明:在2—100μg/L的线性范围内,氟吡菌、烯肟菌、氯虫苯甲酰的峰面积与其浓度呈良好线性关系,方法检出限为2μg/kg;在水稻、西瓜、青菜、番茄和黄瓜5种基质中,10μg/kg、20μg/kg和40μg/kg三个添加水平下,氟吡菌、烯肟菌、氯虫苯甲酰胺回收率为88. 2%—107. 6%,相对标准偏差为1. 2%—8. 2%。该方法可以满足植物源性食品中氟吡菌、烯肟菌、氯虫苯甲酰残留检测的需要。
        The liquid chromatography-tandem mass spectrometry( LC-MS/MS) was developed to analyze fluopicolide,fenaminstrobin and chlorantraniliprole residues in plant foods. After extracted from sample with acetonitrile and cleaned up by dispersive solid-phase extraction with PSA and C18,fluopicolide,fenaminstrobin and chlorantraniliprole was determined by LC-MS/MS. As a result,The calibration curves showed good linearity over the concentration range of 2. 0—100 μg/L with correlation eoefficients above 0. 998,and the limits of determination( LOD) was 2. 0 μg/kg. The recoveries of fluopicolide,fenaminstrobin and chlorantraniliprole residues in plant foods were in the range of 88. 2% —107. 6% at three spiked levels( 10 μg/kg,20 μg/kg,40 μg/kg),and the relative standard deviations were 1. 2% —8. 2%.
引文
[1]杨玉霞,劳水兵,周其峰,等.果蔗中氯虫苯甲酰残留检测方法研究[J].现代农药,2017,16(1):43-46.
    [2]秦冬梅,秦旭,徐应明,等.土壤和番茄中氯虫苯甲酰的残留检测与消解动态研究[J].农业环境科学学报,2010,29(5):858-863.
    [3]张小军,张宗俭,刘尚钟,等.氟吡菌原药的高效液相色谱分析[J].农药,2011,50(9):661-662.
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    [5]张云,郑敬峰,李耀平,等.液相色谱-串联质谱法测定动物源性食品中氯虫苯甲酰和氟虫酰残留量[J].食品科学,2013,34(10):272-275.
    [6]陈靓,井乐刚.基于超高效液相色谱串联质谱法的番茄果实和土壤中氟吡菌残留测定[J].安全与环境学报,2017,17(1):341-345.
    [7]樊晓青,占绣萍,马琳.分散固相净化-气相色谱法检测蔬菜中氟吡菌等15种农药残留[J].现代农药,2014(1):41-43.
    [8]丁立平,方祥,吴文凡.固相萃取-气相色谱-质谱联用法测定蔬菜中烯肟菌的残留及其裂解机理[J].农药学学报,2013,15(6):661-666.

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